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Alliance of Genome Resources

Alliance of Genome Resources is a gene dataset, which contains curated genome information essential for the understanding of the genetics and genomic basis of human biology, health and disease. All data is retrieved from six major model organism databases and the Gene Ontology including FlyBase, Mouse Genome Database (MGI), Rat Genome Database (RGD), Saccharomyces Genome Database (SGD), WormBase, Zebrafish Information Network (ZFIN), and the GO Consortium. In GlyCosmos, only glycan-related disease information has been extracted from Alliance of Genome Resources.

Source Last Updated
Alliance of Genome Resources October 9, 2024
Displaying entries 11376 - 11400 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID ▲ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:0111222 centronuclear myopathy 5 HGNC:16901 Homo sapiens (human) 10290 SPEG
  • RGD:7240710
DOID:0112133 severe congenital neutropenia 3 HGNC:16915 Homo sapiens (human) 10456 HAX1
  • RGD:7240710
DOID:0050590 severe congenital neutropenia HGNC:16915 Homo sapiens (human) 10456 HAX1
  • MGI:6194238
DOID:9743 diabetic neuropathy HGNC:1692 Homo sapiens (human) 967 CD63
  • PMID:10547212
DOID:3407 carotid artery disease HGNC:1692 Homo sapiens (human) 967 CD63
  • PMID:15817881
DOID:10283 prostate cancer HGNC:16921 Homo sapiens (human) 116986 AGAP2
  • PMID:19176382
DOID:0050888 syndromic intellectual disability HGNC:16921 Homo sapiens (human) 116986 AGAP2
  • MGI:6194238
DOID:0050866 oral squamous cell carcinoma HGNC:16921 Homo sapiens (human) 116986 AGAP2
  • PMID:26464646
DOID:1969 cerebral palsy HGNC:16922 Homo sapiens (human) 116987 AGAP1
  • MGI:6194238
DOID:0050888 syndromic intellectual disability HGNC:16922 Homo sapiens (human) 116987 AGAP1
  • MGI:6194238
DOID:526 human immunodeficiency virus infectious disease HGNC:1693 Homo sapiens (human) 968 CD68
  • PMID:22797933
DOID:8567 Hodgkin's lymphoma HGNC:1693 Homo sapiens (human) 968 CD68
  • PMID:21071500
  • PMID:23045593
DOID:0050523 adult T-cell leukemia/lymphoma HGNC:1693 Homo sapiens (human) 968 CD68
  • PMID:23557330
DOID:12236 primary biliary cholangitis HGNC:1693 Homo sapiens (human) 968 CD68
  • PMID:21275501
DOID:2938 Epstein-Barr virus infectious disease HGNC:1693 Homo sapiens (human) 968 CD68
  • PMID:21071500
  • PMID:21602260
DOID:2043 hepatitis B HGNC:1693 Homo sapiens (human) 968 CD68
  • PMID:9699943
DOID:684 hepatocellular carcinoma HGNC:1693 Homo sapiens (human) 968 CD68
  • PMID:28656201
DOID:3965 Merkel cell carcinoma HGNC:1693 Homo sapiens (human) 968 CD68
  • PMID:22050913
DOID:2945 severe acute respiratory syndrome HGNC:1693 Homo sapiens (human) 968 CD68
  • PMID:16237152
  • PMID:19635508
DOID:13254 diverticulitis of colon HGNC:1693 Homo sapiens (human) 968 CD68
  • PMID:21553154
DOID:635 acquired immunodeficiency syndrome HGNC:1693 Homo sapiens (human) 968 CD68
  • PMID:16873198
DOID:11429 endometriosis of pelvic peritoneum HGNC:1693 Homo sapiens (human) 968 CD68
  • PMID:19136478
DOID:0080547 metabolic dysfunction-associated steatohepatitis HGNC:1693 Homo sapiens (human) 968 CD68
  • MGI:6194238
  • PMID:21635548
  • PMID:31337151
DOID:0111974 immunodeficiency 59 HGNC:16931 Homo sapiens (human) 10525 HYOU1
  • RGD:7240710
DOID:12930 dilated cardiomyopathy HGNC:16932 Homo sapiens (human) 10529 NEBL
  • PMID:11140941

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Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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